Canonical Allele Identifier: CA715623994

Gene: LOXL1

Linked Data

• dbSNP Id: rs1194631349
• gnomAD v3: 15-73949083-G-A
• gnomAD v4: 15-73949083-G-A
• MyVariant Identifiers: chr15:g.74241424G>A (hg19) ; chr15:g.73949083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73949083G>A , CM000677.2:g.73949083G>A	GRCh38
NC_000015.9:g.74241424G>A , CM000677.1:g.74241424G>A	GRCh37
NC_000015.8:g.72028477G>A	NCBI36
NG_011466.1:g.27636G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261921.8:c.1603-376G>A MANE Select	ENSP00000261921.7:n.1603-376G>A
ENST00000261921.7:c.1603-376G>A	ENSP00000261921.7:n.1603-376G>A
ENST00000562548.1:n.688-376G>A
ENST00000566011.5:c.*491-376G>A	ENSP00000457827.1:n.*491-376G>A
ENST00000566530.1:n.441-376G>A
ENST00000567675.1:n.76-376G>A
NM_005576.2:c.1603-376G>A	NP_005567.2:n.1603-376G>A
XR_931824.1:n.2120-376G>A
NM_005576.3:c.1603-376G>A	NP_005567.2:n.1603-376G>A
XM_017022179.1:c.556-376G>A	XP_016877668.1:n.556-376G>A
XR_931824.2:n.2109-376G>A
NM_005576.4:c.1603-376G>A MANE Select	NP_005567.2:n.1603-376G>A